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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1375702Erstellt: 25. Oktober 2026

Rofecoxib → (2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diol

https://huagongshe.com/reaction/1375702

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktRofecoxibHCID 5090—
EduktDiisobutylaluminum hydrideHCID 14487—
EduktSodium HydroxideHCID 14798—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2Z)-2-[4-(methylsulfonyl)phenyl]-3-phenylbut-2-ene-1,4-diolHCID 5743477398,7%

Reaktionsschritte

To a solution of 110 g of 4-(4-methanesulfonyl-phenyl)-3-phenyl-5H-furan-2-one in 1.5 L of dichloromethane stirred at −78° C., 150 mL of DIBAL was added dropwise. The resulting mixture was warmed to room temperature and stirred overnight. The reaction mixture was then cooled to −78° C., and 1.2 L of 1 M aqueous NaOH was added dropwise. After the addition, the resulting mixture was warmed to room temperature and the organic phase was separated. The aqueous phase was extracted with dichloromethane. The organic phases were combined and dried over Na2SO4. 110 g of the titled compound was obtained after evaporation. 1H NMR (acetone-d6, 500 M Hz): δ 7.69 (d, 2H), 7.36 (d, 2H), 7.16–7.05 (m, 5H), 4.66 (d, 2H), 4.63 (d, 2H), 4.19 (t, 1H, OH), 4.17 (t, 1 H. OH), 3.04 (s, 3H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07169809B2
Quelldatensatzuspto-grants-2007_01
ORD IDord-5edd1a315fdf4ebbb46c36c2676df4c7
Quellennotizuspto-grants-2007_01